Dating Someone With Klinefelter Syndrome: Despite it being the most common sex chromosomal disorder, its diagnosis is easily missed
Klinefelter syndrome (KS) is a chromosomal disorder affecting males, with the typical karyotype of 47,XXY due to a supernumerary X chromosome, which causes progressive testicular failure resulting in androgen deficiency and infertility.
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1 Epidemiological studies demonstrate that KS is associated with . The clinical phenotype of KS was first described by American physician Dr. Klinefelter syndrome is a genetic condition affecting males, and it often isn't diagnosed until adulthood.
Between 1 in 500 and 1 in 1,000 boys are born with Klinefelter's syndrome (KS).
When an embryo forms, its biological sex develops depending on chromosomes received from each parent.
It is named after Dr. Speech and physical therapy.
Klinefelter syndrome is a genetic condition in which a boy is born with an extra X chromosome.
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The precise genetic etiology of supernumerary X chromosomes (47,XXY) was identified in 1959. One in 550 boys and men have Klinefelter syndrome, yet it often goes undiagnosed. The term “Klinefelter syndrome,” or KS, describes a set of features that can occur in a male who is born with an extra X chromosome in his cells. There are 2 types of chromosome, called the sex chromosomes, that determine the genetic sex of a baby. It is possible that an XXY male could get a woman pregnant naturally. [1] The syndrome describes males with tall stature, small testes, gynecomastia, and azoospermia.
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